Liu Xinhua, Chen Xing, Fei Yifan, Zhang Jiamin, Yue Ouyang, Wang Xuechuan, Jiang Huie
Institute of Biomass & Functional Materials, Shaanxi University of Science &Technology, Xi'an, 710021, China.
College of Bioresources Chemical and Materials Engineering, Shaanxi University of Science & Technology, Xi'an, 710021, China.
Adv Healthc Mater. 2025 Jan;14(3):e2403579. doi: 10.1002/adhm.202403579. Epub 2024 Dec 4.
Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by synovitis, bone-erosion, and joint-destruction. Here, we developed a locally injectable, ROS-scavenging, and ROS-/pH-responsive drug-delivery platform (HC@PTM) by bio-compositing of aldolizing hyaluronic acid (HA) crosslinked with chitosan (CS), and ROS-triggered/eliminated micelles (PTM) coupled with the drug methotrexate(MTX). The PTM efficiently eradicate excessive ROS in RA-joints, precisely triggering drug-release within inflamed arthritic-sites and further confer exceptional antioxidant origins to HC@PTM. HC@PTM with outstanding shape-adaptability and self-repairing properties effectively conformed to irregular articular cartilage while resisting joint-induced deformations. Further, the platform's pH-responsive nature enables on-demand drug-release within acidic inflamed synovium, serving as a drug-reservoir for precise and sustained therapeutic effects. Extensive in vitro and in vivo investigations confirm HC@PTM's ability to induce M2 macrophage polarization, downregulate inflammatory factor expression, and ameliorate the RA-microenvironment, ultimately achieving synergistic therapeutic outcomes. This study represents significant advancements in precise and long-term RA-treatment through a minimally invasive approach, offering potential strategies for novel precision medicine.
类风湿性关节炎(RA)是一种慢性自身免疫性疾病,其特征为滑膜炎、骨侵蚀和关节破坏。在此,我们通过将与壳聚糖(CS)交联的醛醇化透明质酸(HA)进行生物复合,并将ROS触发/消除的胶束(PTM)与药物甲氨蝶呤(MTX)偶联,开发了一种局部可注射、ROS清除且对ROS/pH响应的药物递送平台(HC@PTM)。PTM能有效清除RA关节中过量的ROS,精确触发炎症性关节炎部位的药物释放,并进一步赋予HC@PTM卓越的抗氧化特性。HC@PTM具有出色的形状适应性和自我修复性能,能有效贴合不规则的关节软骨,同时抵抗关节引起的变形。此外,该平台的pH响应特性使其能够在酸性炎症滑膜内按需释放药物,作为一个药物储存库,实现精确且持续的治疗效果。广泛的体外和体内研究证实,HC@PTM能够诱导M2巨噬细胞极化,下调炎症因子表达,改善RA微环境,最终实现协同治疗效果。这项研究代表了通过微创方法在精确和长期RA治疗方面取得的重大进展,为新型精准医学提供了潜在策略。